Global Clinical Trial Manager — Lead Study Operations

Parexel; Columbus (OH); On-site; USD 95,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Trial Manager to lead study-level activities, including document management, vendor oversight, and country/regional operational delivery. You will align feasibility strategies, target setting, risk reviews, and address country challenges impacting delivery.

Responsibilities include overseeing CROs/vendors, budgets, timelines, and regulatory document flow, while contributing to recruitment plans and training materials for compound and protocol levels.

Qualifications

• Minimum 5+ years of clinical research experience gained with a CRO, biotech or pharmaceutical company working on phase I-IV global clinical trials.
• 2-3 years leading aspects of global clinical trials and experience working with CROs.
• Bachelor's degree is required.

Responsibilities

• Manage execution of study-level activities including creating/updating trial-specific documents and country/regional CRO delivery oversight.
• Oversee study sites, regulatory submissions, drug supply, enrollment, and timelines with budget and metrics tracking.
• Provide input on trial-level operational strategies from protocol design to final study report and recruitment plans.
• Identify CRO/vendor opportunities and manage day-to-day CRO/vendor relations and budgets.
• Create/update critical trial documents and support training material development.

Skills

Decision making

Leadership

Global collaboration

Mentoring

Organizational skills

Problem solving

Project management

Communication

MS Office

Travel readiness

Education

Bachelor's degree

Tools

MS Office Suite

Job description

Parexel is seeking a Clinical Trial Manager to lead study-level activities, including document management, vendor oversight, and country/regional operational delivery. You will align feasibility strategies, target setting, risk reviews, and address country challenges impacting delivery.

Responsibilities include overseeing CROs/vendors, budgets, timelines, and regulatory document flow, while contributing to recruitment plans and training materials for compound and protocol levels.